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Synergetics

FDA UDI

Class I (US FDA UDI)

by Synergetics Usa, Inc.

Identity

Trade Name
Synergetics FDA UDI
Generic Name
Ophthalmic soft-tissue manipulation forceps, probe-like, reusable FDA UDI
Device Name
23ga Diamond Black™ Straight Scissors FDA UDI
Model / Reference
23.29.23 FDA UDI
Description
23ga Diamond Black™ Straight Scissors FDA UDI

Identifiers

Catalog Number
23.29.23 FDA UDI
Primary DI / UDI-DI
10841305104300 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Ophthalmic soft-tissue manipulation forceps, probe-like, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ophthalmic soft-tissue manipulation forceps, probe-like, reusable

Synergetics by Synergetics Usa, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic soft-tissue manipulation forceps, probe-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0c00864a-a554-437e-9f0e-5225c0706dd8 35 fields · synced May 31, 2026